Electrochemical aptasensor for thrombin based on polyfunctionalized dendritic nanodevice as natural enzyme-free labeling element

A novel dendritic hybrid nanomaterial with biorecognition and catalytic properties was synthesized by covalent attachment of specific aptamers on the surface of poly(amidoamine) G-4.5 dendrimers and further in situ growth of Pt nanoparticles encapsulated into the polymeric cavities. This nanodevice...

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Bibliographic Details
Authors: Villalonga, Anabel; Fera, Mihai Cristian; Piedras, Alicia; Sánchez Sánchez, Alfredo; Vilela García, Diana; Ojeda Fernández, Irene; Belacortu, Yaiza; Martínez Ruiz, María Paloma; Villalonga Santana, Reynaldo
Format: Article
Publication date:2025
Country:España
Institution:Universidad Complutense de Madrid (UCM)
Repository:Docta Complutense
Language:English
OAI Identifier:oai:docta.ucm.es:20.500.14352/129439
Online Access:https://hdl.handle.net/20.500.14352/129439
Access Level:Open access
Keyword:54
Electrochemical biosensor
Dendrimer
Thrombin
Aptamer
Natural enzyme-free detection
Platinum nanoparticles
Química
2301 Química Analítica
Description
Summary:A novel dendritic hybrid nanomaterial with biorecognition and catalytic properties was synthesized by covalent attachment of specific aptamers on the surface of poly(amidoamine) G-4.5 dendrimers and further in situ growth of Pt nanoparticles encapsulated into the polymeric cavities. This nanodevice was employed as natural enzyme-free labeling element to design an amperometric aptasensor with sandwich-type architecture for the specific detection of thrombin, by using screen-printed carbon electrodes functionalized with Au nanoparticles and capture aptamers as transduction interface. The aptasensor was employed to detect the cardiovascular biomarker in the broad range from 1.0 pM to 1.5 nM, with detection limit of 200 fM. This electroanalytical device also showed high specificity, reproducibility and stability, retaining 92 % of its initial biosensing capacity after 50 days of storage at 4ºC. The aptasensor was successfully employed to quantify thrombin in spiked human serum samples.